If you’re planning on selling your product in China, click here to read the CCC Frequently Asked Questions page. There are no CCC testing facilities outside of China. The China Compulsory Certification (CCC) is required for some products exported to China, mostly electrical and electronic products. One of the organization’s chief activities is ensuring safety in electrical and electronic products by devising technical regulations as national and international standards, then testing to those standards and issuing certifications.
standards written or administered by CSA, UL, the American National Standards Institute (ANSI), NSF International and other organizations.Ī similar agency, VDE Testing and Certification Institute, exists in Europe. They are accredited by OSHA and are an NRTL, and can test products against U.S. Most Class II devices require Pre-market Notification 510(k), while most Class III devices must have Premarket Approval.Ĭanadian Standards Association (CSA) Group provides third-party testing and certification for products sold in North America. The device classification regulation defines the regulatory requirements for a general device type. implantable devices or mechanical heart valves). Food and Drug Association (FDA) requires approval on certain products which are classified into Class I (low risk, such as tongue depressors or exam gloves), Class II (moderate risk, like dialysis equipment or catheters) and Class III (high risk, e.g. The UL and ETL marks prove that the product has met the minimum requirements of established and accepted product safety standards, and that the manufacturer agrees to periodic inspections verifying continued compliance with the standards. The two labs - UL and ETL - provide very similar product testing services, and both are certified NRTL. ETL is administered by Intertek, a global Total Quality Assurance provider. In fact, consumers have come to expect the UL mark on products, and manufacturers tout it when it comes to marketing their products.Įlectrical Testing Labs (ETL) provides similar certification. It is a highly respected third-party testing entity whose sole purpose is to ensure consumer safety. Probably the most recognized testing lab is Underwriters Laboratory (UL). If you’re developing a product, you only want testing at an NRTL. These independent labs test products to the specifications of recognized, applicable safety standards. The Occupational Safety and Health Administration (OSHA) qualifies independent laboratories referred to as Nationally Recognized Testing Laboratories (NRTL). If you don't already have UL, ETL or other certifications before you engage a contract manufacturer, the contract manufacturer will ask these and many other questions to help you determine which certification mark your product needs.
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Industrial components – must meet building codes (Examples: Support beams for load capacity, building materials for mold resistance, water resistance - even zip ties must meet flame retardancy standards).
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Here are some product categories that require testing and certification: Requirements vary from state to state, and insurer to insurer. Some industry standards focus on safety, while others relate to the product’s function and durability. Whether your product requires a certification mark is dependent on the product’s use, and any factors to which it might be subject that could compromise its performance, for example extreme temperatures, direct sunlight or threat of fire. Do I Need to Get a Certification Mark for my Product? In this global economy, it’s imperative that you understand the types of tests that are required wherever you intend to sell your product. Third-party testing and certification is time-consuming and expensive, but it's often a necessary step in product development. In terms of liability, the mark protects you just as much as the consumer, and that's not a "racket." Not only do consumers expect a UL mark, in some cases there are federal and state regulations that require it. As for UL, try selling your kitchen appliance without it. Going for FDA approval for a product that doesn’t require it might seem like overkill, unless the market expects it. Is there any value in seeking FDA approval for a product that doesn’t require FDA approval? Is a UL mark necessary? Isn't all this certification just a racket? Have you ever heard these questions or asked them yourself? You’re not alone.
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